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Stands on its own.
Nothing else here links to this position yet — but the page above is the point: what the
research found, what each genotype means, and where it came from, in language you can
read. Links to conditions, drugs and the senses appear automatically if we write them.
What the study found
Who was studied 3,566 European ancestry individuals; replicated in 4,680 European ancestry individuals.
The effect
The reported allele is A; the catalogue records no effect size
; p = 5 × 10−16.
How common The A allele had a frequency of about 21% in the people studied.
Where it sits Chromosome 7, band 7p14.1 — in an intron of GLI3.
What each result means
A/ATwo copies of the version the research linked to Facial morphology (segment 22). That is the strongest link of the three results. A link in a study is not a diagnosis.
A/TOne copy of the version the research linked to Facial morphology (segment 22). That is a smaller link than two copies.
T/TNo copy of the version the research linked to Facial morphology (segment 22). This is the starting point the study compared everyone against.
Nature genetics · 2021 · PMID 33288918 · open access
Questions about rs62443772
What is rs62443772?
rs62443772 is a single position in the genome, in or near the GLI3 gene. Published research associates it with facial morphology (segment 22). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs62443772 mean I will get this?
No. Common variants like this one move a probability slightly and, on their own, rarely decide anything about one person. Nothing on this page is a diagnosis, and health decisions should be made with a clinician who can see your whole picture.
Where does the information about rs62443772 come from?
GWAS Catalog, Nature genetics 2021, PMID:33288918. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
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